Colon Cancer: Gene >> NANOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229307
Start	7794810:7794810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>T
AA Mutation	p.Gln211His(p.Q211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229307
Start	7794748:7794748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Gly191Arg(p.G191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229307
Start	7794527:7794527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485G>T
AA Mutation	p.Ser162Ile(p.S162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229307
Start	7793125:7793125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000229307
Start	7789711:7789711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97G>T
AA Mutation	p.Glu33Ter(p.E33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229307
Start	7789639:7789640(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.28dupA
AA Mutation	p.Ser10LysfsTer6(p.S10Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NANOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229307
Start	7793041:7793041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243G>T
AA Mutation	p.Glu81Asp(p.E81D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript